Evidence map›Paper›PMID 36203122›Full record

ArticleBMC cancer2022

Circulating levels of PCSK9, ANGPTL3 and Lp(a) in stage III breast cancers.

Emilie Wong Chong, France-Hélène Joncas, Nabil G Seidah, Frédéric Calon, Caroline Diorio, Anne Gangloff

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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  17. Prognostic Value ofCancers · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Emilie Wong ChongFaculty of Medicine, Laval University, Quebec City, QC, Canada.
France-Hélène JoncasOncology Research Axis, CHU de Québec-Laval University Research Center, Quebec City, QC, Canada.
Nabil G SeidahLaboratory of Biochemical Neuroendocrinology, Institut de Recherches Cliniques de Montréal, Montreal, QC, Canada.
Frédéric CalonFaculty of Pharmacy, Laval University, Quebec City, QC, Canada.
Caroline DiorioFaculty of Medicine, Laval University, Quebec City, QC, Canada.
Anne GangloffFaculty of Medicine, Laval University, Quebec City, QC, Canada. Anne.gangloff.1@ulaval.ca.
Université Laval · CAHôpital du Saint-Sacrement · CAMontreal Clinical Research Institute · CA

Funding

This project was funded with an establishment grant for new investigators of the Oncology research axis from the CHU de Québec. NA
6 · The paper itself

Abstract

background / synopsisCholesterol and lipids play an important role in sustaining tumor growth and metastasis in a large variety of cancers. ANGPTL3 and PCSK9 modify circulating cholesterol levels, thus availability of lipids to peripheral cells. Little is known on the role, if any, of circulating lipid-related factors such as PCSK9, ANGPTL3 and lipoprotein (a) in cancers. OBJECTIVE/PURPOSE: To compare circulating levels of PCSK9, ANGPTL3, and Lp(a) in women with stage III breast cancer versus women with premalignant or benign breast lesions.

methodsTwenty-three plasma samples from women diagnosed with a stage III breast cancer (ductal, lobular or mixed) were matched for age with twenty-three plasma samples from women bearing premalignant (stage 0, n = 9) or benign (n = 14) breast lesions. The lipid profile (Apo B, total cholesterol, HDL cholesterol and triglycerides levels) and Lp(a) were measured on a Roche Modular analytical platform, whereas LDL levels were calculated with the Friedewald formula. ANGPTL3 and PCSK9 plasma levels were quantitated by ELISA. All statistical analyses were performed using SAS software version 9.4.

resultsPCSK9 levels were significantly higher in women with stage III breast cancer compared to age-matched counterparts presenting a benign lesion (95.9 ± 27.1 ng/mL vs. 78.5 ± 19.3 ng/mL, p < 0.05, n = 14). Moreover, PCSK9 levels positively correlated with breast disease severity (benign, stage 0, stage III) (Rho = 0.34, p < 0.05, n = 46). In contrast, ANGPTL3 and Lp(a) plasma levels did not display any association with breast disease status and lipids did not correlate with disease severity.

conclusionIn this small cohort of 46 women, PCSK9 levels tended to increase with the severity of the breast disease. Given that PCSK9 plays an important role in maintaining cholesterolemia, and a potential role in tumor evasion, present results warrant further investigation into a possible association between PCSK9 levels and breast cancer severity in larger cohorts of women.

Indexed as

Breast NeoplasmsProprotein Convertase 9Angiopoietin-Like Protein 3Angiopoietin-like ProteinsApolipoproteins BCholesterolCholesterol, HDLFemaleHumansLipoprotein(a)TriglyceridesAngiopoietin-Like Protein 3Angiopoietin-like ProteinsANGPTL3 protein, humanApolipoproteins BCholesterolCholesterol, HDLLipoprotein(a)PCSK9 protein, humanProprotein Convertase 9TriglyceridesANGPTL3Breast cancerCancer progressionEndogenous lipid metabolismLipoprotein(a)PCSK9

Identifiers

PMID36203122
PMCPMC9535963
OpenAlexW4302293089

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.